Stimulation of the Adenosine 3′,5′-Monophosphate and the Ca2+Messenger Systems Together Reverse Dopaminergic Inhibition of Prolactin Release*

Abstract

Dopaminergic inhibition of PRL [prolactin] release stimulated by agents that affect cytosolic Ca2+ concentrations, C-kinase activity and cAMP levels was studied in perifused rat anterior pituitary cells cultured on cytodex beads. A23187 [calcimycin] (20 .mu.M) was used to increase intracellular Ca2+, the phorbol ester 12-O-tetradecanoyl-phorbol-13-acetate (TPA; 50 nM) to stimulate C-kinase, forskolin (10 .mu.M) to increase intracellular cAMP, and 8-bromo-cAMP to mimic cAMP. Dopamine (10 .mu.M) inhibited PRL release to 20-60% of the basal release within 10 min. After 30 min of preincubation with dopamine, the absolute amount of release sitmulated by 100 nM TRH was strongly inhibited, although the pattern of release, a quick burst followed by sustained release at a lower rate, was the same in the presence or absence of dopamine. A23187 (20 .mu.M) caused a rapid burst of PRL release that subsided within 10 min; and TPA (50 nM) caused a sustained release that began within 4 min anbd continued for at least 30 min. TPA and A23187 combined caused a rapid burst of release followed by a sustained phase of release similar to that caused by TRH. Preincubation with dopamine inhibited the absolute amount of PRL release caused by A23187 alone, TPA alone, or the 2 combined, although, as with TRH, the pattern or release remained the same. Forskolin (1 or 10 .mu.M) or 8-bromo-cAMP (3 mM) induced a 1.5- to 2-fold increase in PRL release this was completely prevented by dopamine. Preincubation with both dopamine and 8-bromo-cAMP or forskolin restored the amount of release stimulated by TPA alone or TPA and A23187 in the presence of dopamine to the level of release sitmulated by these agents in the absence of dopamine. Therefore, activating either the cAMP messenger system or the Ca2+ system alone will no abolish dopaminergic inhibition, but activating the 2 together will. Apparently dopamine blocks release by inhibiting both adenylate cyclase and a step in the Ca2+ messenger system.